35377-19-6 Usage
Uses
Used in Organic Chemistry:
1-(3-phenylprop-2-en-1-ylidene)-1H-indene is used as a precursor in the synthesis of various organic compounds, leveraging its unique chemical structure and reactivity for the creation of a wide range of products.
Used in Material Science:
Due to its distinctive properties, 1-(3-phenylprop-2-en-1-ylidene)-1H-indene is utilized as a starting material in the development of new materials with potential applications in various industries.
Used in Pharmaceutical Production:
1-(3-phenylprop-2-en-1-ylidene)-1H-indene may also serve as a starting material in the production of pharmaceuticals, contributing to the development of new drugs and treatments.
Used in Agrochemical Production:
Similarly, 1-(3-phenylprop-2-en-1-ylidene)-1H-indene is used as a starting material in the creation of agrochemicals, potentially leading to advancements in agriculture through the development of new products.
Check Digit Verification of cas no
The CAS Registry Mumber 35377-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,7 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35377-19:
(7*3)+(6*5)+(5*3)+(4*7)+(3*7)+(2*1)+(1*9)=126
126 % 10 = 6
So 35377-19-6 is a valid CAS Registry Number.
35377-19-6Relevant academic research and scientific papers
A Rapid and Highly Efficient Method for the Synthesis of Benzofulvenes via CsOH-Catalyzed Condensation of Indene and Aldehydes
Yi, Rongnan,Chen, Jinyang,Wang, Xueyan,Liang, Zhiwu,Xu, Xinhua
supporting information, p. 1347 - 1351 (2018/04/02)
A fast condensation of indene with a wide range of aldehydes catalyzed by cesium hydroxide monohydrate (CsOH·H2O) for the synthesis of benzofulvenes with good to excellent yields was demonstrated. The condensation can be completed within a few minutes under room temperature and air atmosphere without the use of special ligands or phase-transfer catalysts. In addition, the ratio of indene to aldehydes played an important role in this reaction. The single condensation products 3 can be obtained as main products with a ratio of 1.2:1, whereas the double condensation products 4 can be obtained by changing the ratio to 1:2.2. This protocol provides an efficient, simple and general method for the synthesis of benzofulvenes 3 and double condensation products 4, which are important intermediates in the synthesis of numerous drugs and natural products.
